Canonical Allele Identifier: CA2036511498
Gene: KRT75 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433841G= , CM000674.2:g.52433841G= GRCh38
NC_000012.11:g.52827625G= , CM000674.1:g.52827625G= GRCh37
NC_000012.10:g.51113892G= NCBI36
NG_008403.1:g.5486C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.464C= MANE Select ENSP00000252245.5:p.Thr155=
ENST00000252245.5:c.464C= ENSP00000252245.5:p.Thr155=
NM_004693.2:c.464C= NP_004684.2:p.Thr155=
NM_004693.3:c.464C= MANE Select NP_004684.2:p.Thr155=
Search 100 bp 5'
Search 100 bp 3'